BEUDAMED
    5 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ENDOTAK RELIANCE G

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code LWS·November 11, 2008

    SECURE ACUTE CARE BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·August 10, 2011

    ALARIS PUMP MODULE

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP·Product code FRN·July 17, 2013

    13X75 MM 4.0 ML BD VACUTAINER® PLUS PLASTIC WHOLE BLOOD TUBE

    FDA Adverse Event
    Injury ·BECTON, DICKINSON & CO.·Product code JKA·July 25, 2017

    13X75 MM 4.0 ML BD VACUTAINER® PLUS PLASTIC WHOLE BLOOD TUBE

    FDA Adverse Event
    Injury ·BECTON, DICKINSON & CO.·Product code JKA·July 25, 2017